ANTI-PHENACETIN MONOCLONAL ANTIBODY HYBRIDOMA CELL STRAIN AD AND ITS PREPARATION METHOD AND APPLICATION

Abstract

The invention discloses an anti-phenacetin monoclonal antibody hybridoma cell strain AD, a preparation method and application thereof, and relates to the technical field of food safety immunodetection. The monoclonal antibody hybridoma cell strain is named monoclonal cell strain AD and the number CGMCC19681. The Phe-BA obtained by the hydrolysis of the reaction product of the phenacetin metabolite acetaminophen and ethyl 4-bromobutyrate is used as the hapten, and the hapten is coupled with the carrier protein to prepare the immunogen Phe-BA-BSA. After the mice were immunized with the immunogen Phe-BA-BSA, they were fused with myeloma cells by PEG method, screened by indirect competitive enzyme-linked immunosorbent assay and subcloned five times to obtain hybridoma cell lines. The monoclonal antibody secreted by the cell line can be made into a phenacetin detection kit, which has good affinity and detection sensitivity for phenacetin, and can be used for immunodetection of phenacetin residues in food.

Claims

1. A hybridoma cell strain AD with anti-phenacetin monoclonal antibody, deposited at the China General Microbiological Culture Collection Center with Access Number CGMCC No. 19681.

2. A method of preparing the hybridoma cell strain AD according to claim 1 comprising: immunizing mice with phenacetin complete antigen through cell fusion and culturing in HAT selective medium to establish the hybridoma cell strain AD, and immunizing mice with Phe-BA-BSA immunogen to obtain phenacetin complete antigen-immunized mice.

3. The method of claim 2, wherein the complete phenacetin antigen is obtained by coupling a Phe-BA hapten with a carrier protein, wherein the carrier protein includes bovine serum albumin (BSA) and ovalbumin (OVA); phenacetin immunogens include Phe-BA-BSA, Phe-BA-OVA, the Phe-BA hapten is obtained by hydrolysis of the product of the reaction between acetaminophen and ethyl 4-bromobutyrate, the structural formula of the Phe-BA hapten is as follows: ##STR00003##

4. The method of claim 3, wherein the preparation method of the Phe-BA hapten is as follows: calculate by molar ratio: dissolve 1 equ. acetaminophen in dimethyl sulfoxide, then add 4-6 equ. K.sub.2CO.sub.3, add 2-5 equ. ethyl 4-bromobutyrate under stirring, and heat to reflux at about 100° C. (80˜120° C.), when the reaction is complete, the mixture is cooled down to room temperature and concentrated, the NaOH solution was added into the concentrated solution, the mixture is heated to 70˜80° C. under stirring for reaction, then, the pH of the mixture was adjusted to 4˜5 with HCl when the solution is cooled down to room temperature, the solution is then extracted and purified, a white solid obtained and dried, which is the hapten Phe-BA.

5. The method of claim 2, wherein the immunization method of the phenacetin-immunized mice is to inject BALB/c mice subcutaneously through the back of the neck, and firstly immunize for the first time with an equal volume mixed emulsion of Freund's complete adjuvant and phenacetin immunogen as an injection; then, several booster immunizations were carried out with an equal volume of mixed emulsion of incomplete Freund's adjuvant and phenacetin immunogen as an injection; the last immunization was performed with 50 μL of phenacetin immunogen diluted to 0.5 mg/mL in normal saline.

6. The method of claim 2, wherein an injection dose of the first immunization is 100 ag/only, an injection dose of each booster is 50 μg/only, and an injection dose of the sprint immunization is 25 μg/only; the interval between the first immunization and the first booster immunization is one month; there are 21 days between the booster immunizations; the booster immunizations are performed 4 to 6 times.

7. The method of claim 2, wherein the splenocytes of phenacetin-immunized mice are fused with myeloma cells by polyethylene glycol method, cultured in HAT medium, and positive cell wells are detected by indirect ELISA, the inhibitory effect of the positive cell wells is further determined by icELISA, and the positive cell wells with the best inhibition are subcloned three times by limiting dilution method, and the hybridoma cell line AD is obtained by screening finally.

8. Anti-phenacetin monoclonal antibody secreted by the monoclonal hybridoma cell strain AD according to claim 1.

9. A method for analysis and detection of phenacetin residues in food safety detection comprising adding the anti-phenacetin monoclonal antibody of claim 8 in a subject to form a detection subject, and then analyzing and detecting phenacetin residues in food with the detection subject, wherein the detection subject comprises reagents, detection plates, and kits.

10. (canceled)

Description

BRIEF DESCRIPTION THE DRAWINGS

[0021] FIG. 1 is the subtype identification of monoclonal antibody AD;

[0022] FIG. 2 is the affinity determination of monoclonal antibody AD;

[0023] FIG. 3 is a standard curve for the inhibition of phenacetin by monoclonal antibody AD.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS OF THE INVENTION

[0024] The present invention will be further described below with reference to the accompanying drawings and embodiments.

Example

[0025] The present invention can be better understood from the following examples. However, those skilled in the art can easily understand that the specific material ratios, process conditions and results described in the examples are only used to illustrate the present invention and should not and will not limit the present invention described in detail in the claims.

[0026] In the present invention, the mice immunized with the phenacetin complete antigen are subjected to cell fusion, cultured in a HAT selective medium, and the cell supernatant is screened by icELISA, and finally a monoclonal antibody hybridoma cell strain with high sensitivity to phenacetin is obtained.

[0027] 1. Synthesis of Hapten

[0028] (1) Synthesis of Hapten Phe-BA:

[0029] The synthetic route is as follows:

##STR00002##

[0030] Dissolve 0.20 g of acetaminophen in 2 mL of dimethyl sulfoxide, add 1.0 g of K.sub.2CO.sub.3, and stir for 0.5 h. Then, 0.77 g of ethyl 4-bromobutyrate was added under stirring. The mixture was heated to reflux at 110° C. for 24 h, and monitored by TLC. When the reaction is complete, stop heating and concentrated until the temperature of the reaction solution cooled down to room temperature; Then, 2 mL of 1 mol/L NaOH was added into the above solution, heating to 80° C. for 1 h under stirring. When the temperature calmed down to room temperature, the reaction solution which was adjusted to pH 4 with 1.0 mol L.sup.−1 aqueous HCl., The solution was then washed with ethyl acetate three times, and the organic phase was collected, dried over anhydrous Na.sub.2SO.sub.4 and concentrated., After purification by silica gel column and concentration, a white solid was obtained, that is the hapten Phe-BA.

[0031] 2. Preparation of complete antigen: The hapten Phe-BA prepared in the above step 1 is coupled with bovine serum albumin (BSA) to obtain the complete antigen Phe-BA-BSA.

[0032] The preparation method of the complete antigen Phe-BA-BSA is as follows:

[0033] a. 2.85 mg of the hapten Phe-BA obtained in step (1) was dissolved in 200 μL of anhydrous N,N-dimethylformamide, and then 1.6 mg of 1-ethyl-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDCI) and 1.0 mg of N-hydroxysuccinimide (NHS) were added, and then the mixture was stirred at room temperature for 0.5 h to obtain liquid A. In addition, 10 mg of bovine serum albumin (BSA) was dissolved in 2 mL of boric acid buffer solution to obtain solution B. Then, the solution A was slowly added dropwise to solution B with constant stirring at room temperature for 2 h to obtain a mixture containing Phe-BA-BSA.

[0034] b. Dialysis: The 10 cm dialysis bag was boiled in boiling water for 5 min, rinsed with deionized water at 60° C. for 3 min, and stored in deionized water at 4° C. for later use. The mixed solution containing Phe-BA-BSA in step (a) was placed in a dialysis bag, and 0.01 mol/L PBS was used as the dialysate, dialyzed at 4° C. for 3 d, and the dialysate was replaced three times a day to separate the complete antigen and unconjugated haptens and other small molecules. The complete antigen includes immunogen and coating antigen; wherein, the immunogen Phe-BA-BSA is used for the next step of mouse immunization; the coating antigen is used for the detection in the subsequent step 7.

[0035] In the same way, the complete antigen Phe-BA-OVA is obtained by coupling the hapten Phe-BA and ovalbumin (OVA), including the immunogen and the coating antigen. The immunogen is used for the next step of mouse immunization, and the coating antigen is used for the detection in the subsequent step 7.

[0036] In the present Experimental example, the subsequent immunization and detection-related steps are specifically described by using the immunogen Phe-BA-BSA and the coating original Phe-BA-OVA as examples.

[0037] 3. Immunization of mice: The injection was formed by emulsification of Phe-BA-BSA immunogen mixed with an equal volume of Freund's adjuvant, and subcutaneously injected into BALB/c mice through the back of the neck.

[0038] For the first immunization (100 μg/only), an equal volume of mixed emulsion of Freund's complete adjuvant and phenacetin immunogen was used as an injection. For 5 boosting immunizations, an equal volume emulsion of incomplete Freund's adjuvant and phenacetin immunogen was used as an injection. One month between the first immunization and the first booster immunization, and 21 days between multiple booster immunizations. The last sprint immunization was performed with 50 μL of water diluted to 0.5 mg/mL Phe-BA-BSA immunogen (25 μg/only, no adjuvant). Serum titers and inhibition rates were detected by indirect competitive enzyme-linked immunosorbent assay (icELISA).

[0039] 4. Cell Fusion

[0040] Three days after the rush immunization, cell fusion is carried out according to the conventional PEG method. The specific steps are as follows:

[0041] a. The eyeballs were removed to collect blood, and the Phe-BA-BSA-immunized mice were killed by cervical dislocation, and then immediately put into 75% alcohol for disinfection and soaked for about 5 minutes. The spleen of the mouse was aseptically removed, moderately ground with the tip of a syringe and passed through a 200-mesh cell screen to obtain a spleen cell suspension. The suspension was collected, centrifuged (1200 rpm, 8 min), and the splenocytes were washed three times with RPMI-1640 medium. After the last centrifugation, the splenocytes were diluted to a certain volume, counted, and used for later use.

[0042] b. Collection of murine myeloma SP2/0 cells: 7-10 days before cell fusion, SP2/0 tumor cells were cultured in RPMI-1640 medium containing 10% FBS (fetal bovine serum) in a 5% CO.sub.2 incubator. Before fusion, the number of SP2/0 tumor cells was required to reach 1˜×10.sup.7, to ensure that the SP2/0 tumor cells were in the logarithmic growth phase before fusion. At fusion, tumor cells were collected, suspended in RPMI-1640 basal medium, and counted.

[0043] c. The fusion process was 7 min. The first minute, 1 mL of PEG 1500 was added dropwise to the cells from slow to fast; the second minute, let stand. On the 3rd and 4th minutes, drop 1 mL of RPMI-1640 medium within 1 minute; on the 5th and 6th minutes, dropwise add 2 mL of RPMI-1640 medium within 1 minute; on the 7th minute, every 10 s Add 1 mL of RPMI-1640 medium dropwise. Then, the above cell mixture was placed in a 37° C. warm bath for 5 min, centrifuged (800 rpm, 8 min), and the supernatant was discarded to obtain a precipitate. The solution is centrifuged and then suspended in an RPMI-1640 screening medium containing 20% fetal bovine serum and 2% 50×HAT, and then added to a 96-well cell culture plate and cultured in an incubator at 37° C. in a 5% CO.sub.2 atmosphere.

[0044] 5. Cell Screening and Cell Strain Establishment

[0045] The medium of the fused cells is semi-changed with an RPMI-1640 screening medium on the third day of cell fusion, and then completely changed with an RPMI-1640 transition medium containing 20% fetal bovine serum and 1% 100×HT on the 5th day. The cell supernatant is taken for screening on the 7th day.

[0046] The screening is divided into two steps: the first step is to select positive cell wells by icELISA, the second step is to use the phenacetin as a standard and measure the inhibitory effect of the positive cells by icELISA. Cell wells with a good inhibitory effect to the phenacetin standard are selected and subcloned by a limiting dilution method. The same method is used for detection and repeat three times to obtain a cell strain AD.

[0047] 5. Preparation and Identification of Anti-Phenacetin Monoclonal Antibody

[0048] 8-10 weeks old BALB/c mice are taken and each intraperitoneally injected with 1 mL of sterile paraffin oil, and 7 days later, intraperitoneally injected with a 1×10.sup.6 hybridoma cell strain; ascites is collected from the 7th day and purified by an octanoic acid-ammonium sulfate method. The purified anti-phenacetin monoclonal antibody was finally obtained and stored at −20° C.

[0049] Using the mouse monoclonal antibody subtype identification kit to identify the immunoglobulin subtype of the anti-phenacetin monoclonal antibody purified from ascites, its subtype is IgG2b type, and it was detected by the mouse monoclonal antibody subtype identification kit. The chain type is the kappa type, as shown in FIG. 1.

[0050] The affinity of anti-phenacetin monoclonal antibody determined by indirect ELISA was 5.36×10.sup.8 L/mol, as shown in FIG. 2. The sensitivity to phenacetin was detected by icELISA, as shown in FIG. 3. According to the standard equation y=−0.3479 x+0.6733 (R.sup.2=0.9863), the IC.sub.50 was calculated to be 3.0 μg/L.

[0051] The above results show that the prepared anti-phenacetin monoclonal antibody has high affinity and sensitivity and can be used for phenacetin immunoassay detection and the preparation of affinity columns.

[0052] 7. Antibody Application

[0053] The anti-phenacetin monoclonal antibody prepared by the hybridoma cell strain AD through in vivo ascites was applied to the addition and recovery test of phenacetin, and the specific steps were as follows:

[0054] 7.1 Coating: The coating antigen Phe-BA-OVA obtained in the previous step 2 was diluted to 0.1 μg/mL with 0.05 mol L−1 pH 9.6 carbonate buffer, 100 μL/well, at 37° C. for 2 h.

[0055] 7.2 Washing: The solution in the plate was poured out and washed three times with washing solution, 3 min each time.

[0056] 7.3 Closure: the plate is closed with blocking solution, 200 μL per well, at 37° C. for 2 h; the plate is washed and dried for later use;

[0057] 7.4 Add sample:

[0058] 100 μL of PBS was added to the positive control wells; 100 μL of phenacetin standard solution with a concentration of 0.3˜50 μg/L was added to the detection wells. Then, the anti-phenacetin monoclonal antibody was diluted with 0.01 mol L.sup.−1 PBS to 0.1 g/mL, and added to the coated wells of each dilution, 100 μL/well, and reacted at 37° C. for 30 min; Then the plate is thoroughly washed. 100 μL of HRP-goat anti-mouse IgG diluted at a ratio of 1:3000 is added to each well and reacts at 37° C. for 30 min.

[0059] 7.5 Color rendering: The ELISA plate was taken out, washed thoroughly, added 100 μL of TMB color developing solution to each well, and reacted at 37° C. for 15 min in the dark.

[0060] 7.6 Termination and determination: 50 μL of stop solution was added to each well to stop the reaction, and then the OD450 value of each well was measured with a microplate reader.

[0061] The IC.sub.50 of anti-phenacetin monoclonal antibody determined by icELISA was 3.0 μg/L. It shows that it has high sensitivity to phenacetin and can be used for phenacetin immunoassay detection.

[0062] In the above steps, the configuration of each solution is as follows:

[0063] Carbonate buffer solution (CBS): 1.59 g of Na.sub.2CO.sub.3 and 2.93 g of NaHCO.sub.3 are weighed and separated dissolved in a small amount of double distilled water; the two solutions are mixed; double distilled water is added to the mixed solution till about 800 mL and the mixed solution is mixed to be uniform; the pH is adjusted to 9.6, and double distilled water is added till the mixed solution reaches 1000 mL and the obtained solution is stored at 4° C. for later use.

[0064] Phosphate buffer solution (PBS): 8.00 g of NaCl, 0.2 g of KCl, 0.2 g of KH.sub.2PO.sub.4, 2.9 g of Na.sub.2HPO.sub.4.12 H.sub.2O are dissolved in 800 mL of pure water, the pH is adjusted to 7.2-7.4 with NaOH or HCl, and the solution is maintained at a constant volume of 1000 mL.

[0065] PBST: PBS Containing 0.05% Tween 20.

[0066] TMB developing solution: Solution A: 18.43 g of Na.sub.2HPO.sub.4.12H.sub.2O and 9.33 g of citric acid are added with pure water to 100 mL; B solution: 60 mg of TMB is dissolved in 1000 mL of ethylene glycol. The solution A and the solution B are mixed at a ratio of 1:5 to obtain TMB (a developing solution, mixed when necessary).

[0067] The above is only the preferred embodiment of the invention. It should be pointed out that for ordinary technicians in the technical field, several improvements and refinements can be made without departing from the principle of the invention, and these improvements and refinements should also be regarded as the protection scope of the invention.